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Clinical Trials/NCT03254914
NCT03254914
Completed
Not Applicable

A Multi-center, Cluster-randomized, Prospective, Observational Study

Boryung Pharmaceutical Co., Ltd1 site in 1 country3,554 target enrollmentAugust 9, 2017
ConditionsHypertension

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Hypertension
Sponsor
Boryung Pharmaceutical Co., Ltd
Enrollment
3554
Locations
1
Primary Endpoint
Rate of reaching target blood pressure
Status
Completed
Last Updated
last year

Overview

Brief Summary

The purpose of this study is to evaluate the effect of home blood pressure monitoring on controlling blood pressure and correlation between home blood pressure and clinic blood pressure in hypertensive patients receiving two or more concomitant antihypertensive agents including fimasartan

Detailed Description

A multi-center, cluster-randomized, prospective, observational study

Registry
clinicaltrials.gov
Start Date
August 9, 2017
End Date
February 28, 2019
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Subjects who voluntarily signed informed consent for participating in this clinical study
  • Male and female over the age of 19
  • Hypertensive patients receiving two or more concomitant anti-hypertensive agents including fimasartan

Exclusion Criteria

  • Renal dialysis patients.
  • Diabetic nephropathy patients taking angiotensin-converting enzyme inhibitor.
  • Severe renal disorder
  • Subjects with hereditary disorders of galactose intolerance, Lapp lactase deficiency or glucose-galactose malabsorption.
  • Medical history with hypersensitivity to Fimasartan
  • Pregnant women or lactating female.
  • Participate in another clinical trial.

Outcomes

Primary Outcomes

Rate of reaching target blood pressure

Time Frame: 12 weeks after treatment

Rate of reaching target blood pressure after treatment for 12 weeks

Study Sites (1)

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